| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (splice acceptor variant) | Fanconi anemia complementation group A | |
| | FANCA, LOC132090450 (F1135del) | Microsatellite (inframe_deletion) | Fanconi anemia +1 more | GPathogenic/Likely pathogenic |
| | FANCA, LOC132090450 (A1132fs) | Indel (frameshift variant) | Fanconi anemia complementation group A | |
| | LOC132090450, FANCA (T1131A) | Single nucleotide variant (missense variant) | Fanconi anemia +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene